Canonical Allele Identifier: CA2678148492
Gene: BTNL2 HGNC NCBI
TSBP1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32405417_32405418insGC , CM000668.2:g.32405417_32405418insGC GRCh38
NC_000006.11:g.32373194_32373195insGC , CM000668.1:g.32373194_32373195insGC GRCh37
NC_000006.10:g.32481172_32481173insGC NCBI36
NG_054759.1:g.8462_8463insGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000374993.5:n.137+1627_137+1628insGC (BTNL2)
ENST00000446536.3:c.80-135_80-134insGC (BTNL2) ENSP00000388434.2:n.80-135_80-134insGC
ENST00000454136.8:c.80-132_80-131insGC (BTNL2) MANE Select ENSP00000390613.3:n.80-132_80-131insGC
ENST00000465865.6:c.80-132_80-131insGC (BTNL2) ENSP00000420063.1:n.80-132_80-131insGC
ENST00000544175.3:c.80-132_80-131insGC (BTNL2) ENSP00000443364.2:n.80-132_80-131insGC
ENST00000374993.4:c.80-132_80-131insGC (BTNL2) ENSP00000364132.1:n.80-132_80-131insGC
ENST00000446536.2:c.80-135_80-134insGC (BTNL2) ENSP00000388434.2:n.80-135_80-134insGC
ENST00000454136.7:c.80-132_80-131insGC (BTNL2) ENSP00000390613.3:n.80-132_80-131insGC
ENST00000465865.5:c.80-132_80-131insGC (BTNL2) ENSP00000420063.1:n.80-132_80-131insGC
ENST00000544175.2:c.-229-132_-229-131insGC (BTNL2) ENSP00000443364.1:n.-229-132_-229-131insGC
NM_001304561.1:c.80-132_80-131insGC (BTNL2) NP_001291490.1:n.80-132_80-131insGC
XM_011514755.1:c.80-132_80-131insGC (BTNL2) XP_011513057.1:n.80-132_80-131insGC
XM_011514756.1:c.80-132_80-131insGC (BTNL2) XP_011513058.1:n.80-132_80-131insGC
XM_011515039.1:c.482-37_482-36insGC (TSBP1-AS1) XP_011513341.1:n.482-37_482-36insGC
XR_926699.1:n.104-37_104-36insGC (TSBP1-AS1)
NR_136245.1:n.303-37_303-36insGC (TSBP1-AS1)
XM_017011057.1:c.80-132_80-131insGC (BTNL2) XP_016866546.1:n.80-132_80-131insGC
NM_001304561.2:c.80-132_80-131insGC (BTNL2) MANE Select NP_001291490.1:n.80-132_80-131insGC